Skip to content

Temple Touch Pro (TTP) Non Invasive Continuous Temperature Measurement System

Temple Touch Pro (TTP) Non Invasive Continuous Temperature Measurement System.

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT01489280
Acronym
TTP
Enrollment
800
Registered
2011-12-09
Start date
2012-05-31
Completion date
Unknown
Last updated
2012-09-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Body Temperature During Surgery

Keywords

Temple Touch Pro, Medisim, temperature, surgery

Brief summary

In this study, the body temperatures of men and women undergoing elective surgery will be measured using the Temple Touch Pro. In the operating room, each patient's temperature will be measured with both the Temple Touch Pro and another one or two of the continuous reference methods used clinically for measuring the core temperature. The Medisim Temple Touch Pro thermometer combines a noninvasive, biocompatible patch and a receiving unit. The former is attached to the skin, while the latter is placed near the patient or the vital signs monitor and receives data from the patch. The core temperature equivalent is displayed. The Medisim Temple Touch Pro is based on the measurements made by conductive sensors that perform skin temperature measurements and then applies a special algorithm in order to calculate the body's temperature.

Interventions

None listed

Sponsors

Medisim Ltd
Lead SponsorINDUSTRY

Study design

Observational model
COHORT
Time perspective
RETROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
Yes

Inclusion criteria

The patients will be chosen for the trial if the following criteria are met: * Male and female patients scheduled to undergo cardiothoracic surgery and major (surgeries scheduled to last more than 90 minutes) abdominal, vascular and general surgery. * The surgical procedure requires temperature monitoring. * Informed consent signed by the patient or his legal guardian.

Exclusion criteria

The patients will be excluded from the trial if one of the following occurs: * The medical staff decides that the patient should not participate. * Unavailable measurement site in case of operations performed in the head area.

Countries

Israel

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026